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Exploring Genomic Variations in Nematode-Resistant Mutant Rice Lines

Rice (Oryza sativa) production is seriously affected by the root-knot nematode Meloidogyne graminicola, which has emerged as a menace in upland and irrigated rice cultivation systems. Previously, activation tagging in rice was utilized to identify candidate gene(s) conferring resistance against M. g...

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Autores principales: Dash, Manoranjan, Somvanshi, Vishal Singh, Godwin, Jeffrey, Budhwar, Roli, Sreevathsa, Rohini, Rao, Uma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988285/
https://www.ncbi.nlm.nih.gov/pubmed/35401589
http://dx.doi.org/10.3389/fpls.2022.823372
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author Dash, Manoranjan
Somvanshi, Vishal Singh
Godwin, Jeffrey
Budhwar, Roli
Sreevathsa, Rohini
Rao, Uma
author_facet Dash, Manoranjan
Somvanshi, Vishal Singh
Godwin, Jeffrey
Budhwar, Roli
Sreevathsa, Rohini
Rao, Uma
author_sort Dash, Manoranjan
collection PubMed
description Rice (Oryza sativa) production is seriously affected by the root-knot nematode Meloidogyne graminicola, which has emerged as a menace in upland and irrigated rice cultivation systems. Previously, activation tagging in rice was utilized to identify candidate gene(s) conferring resistance against M. graminicola. T-DNA insertional mutants were developed in a rice landrace (acc. JBT 36/14), and four mutant lines showed nematode resistance. Whole-genome sequencing of JBT 36/14 was done along with the four nematode resistance mutant lines to identify the structural genetic variations that might be contributing to M. graminicola resistance. Sequencing on Illumina NovaSeq 6000 platform identified 482,234 genetic variations in JBT 36/14 including 448,989 SNPs and 33,245 InDels compared to reference indica genome. In addition, 293,238–553,648 unique SNPs and 32,395–65,572 unique InDels were found in the four mutant lines compared to their JBT 36/14 background, of which 93,224 SNPs and 8,170 InDels were common between all the mutant lines. Functional annotation of genes containing these structural variations showed that the majority of them were involved in metabolism and growth. Trait analysis revealed that most of these genes were involved in morphological traits, physiological traits and stress resistance. Additionally, several families of transcription factors, such as FAR1, bHLH, and NAC, and putative susceptibility (S) genes, showed the presence of SNPs and InDels. Our results indicate that subject to further genetic validations, these structural genetic variations may be involved in conferring nematode resistance to the rice mutant lines.
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spelling pubmed-89882852022-04-08 Exploring Genomic Variations in Nematode-Resistant Mutant Rice Lines Dash, Manoranjan Somvanshi, Vishal Singh Godwin, Jeffrey Budhwar, Roli Sreevathsa, Rohini Rao, Uma Front Plant Sci Plant Science Rice (Oryza sativa) production is seriously affected by the root-knot nematode Meloidogyne graminicola, which has emerged as a menace in upland and irrigated rice cultivation systems. Previously, activation tagging in rice was utilized to identify candidate gene(s) conferring resistance against M. graminicola. T-DNA insertional mutants were developed in a rice landrace (acc. JBT 36/14), and four mutant lines showed nematode resistance. Whole-genome sequencing of JBT 36/14 was done along with the four nematode resistance mutant lines to identify the structural genetic variations that might be contributing to M. graminicola resistance. Sequencing on Illumina NovaSeq 6000 platform identified 482,234 genetic variations in JBT 36/14 including 448,989 SNPs and 33,245 InDels compared to reference indica genome. In addition, 293,238–553,648 unique SNPs and 32,395–65,572 unique InDels were found in the four mutant lines compared to their JBT 36/14 background, of which 93,224 SNPs and 8,170 InDels were common between all the mutant lines. Functional annotation of genes containing these structural variations showed that the majority of them were involved in metabolism and growth. Trait analysis revealed that most of these genes were involved in morphological traits, physiological traits and stress resistance. Additionally, several families of transcription factors, such as FAR1, bHLH, and NAC, and putative susceptibility (S) genes, showed the presence of SNPs and InDels. Our results indicate that subject to further genetic validations, these structural genetic variations may be involved in conferring nematode resistance to the rice mutant lines. Frontiers Media S.A. 2022-03-24 /pmc/articles/PMC8988285/ /pubmed/35401589 http://dx.doi.org/10.3389/fpls.2022.823372 Text en Copyright © 2022 Dash, Somvanshi, Godwin, Budhwar, Sreevathsa and Rao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Dash, Manoranjan
Somvanshi, Vishal Singh
Godwin, Jeffrey
Budhwar, Roli
Sreevathsa, Rohini
Rao, Uma
Exploring Genomic Variations in Nematode-Resistant Mutant Rice Lines
title Exploring Genomic Variations in Nematode-Resistant Mutant Rice Lines
title_full Exploring Genomic Variations in Nematode-Resistant Mutant Rice Lines
title_fullStr Exploring Genomic Variations in Nematode-Resistant Mutant Rice Lines
title_full_unstemmed Exploring Genomic Variations in Nematode-Resistant Mutant Rice Lines
title_short Exploring Genomic Variations in Nematode-Resistant Mutant Rice Lines
title_sort exploring genomic variations in nematode-resistant mutant rice lines
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988285/
https://www.ncbi.nlm.nih.gov/pubmed/35401589
http://dx.doi.org/10.3389/fpls.2022.823372
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